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UPTRAVI 800 MCG — DIN 02451182

SELEXIPAG : 800 MCG · JANSSEN INC · TABLET · wholesale supply in Canada

Health Canada status: MARKETED

What is UPTRAVI?

UPTRAVI 800 MCG contains SELEXIPAG : 800 MCG. It is listed in the Health Canada Drug Product Database under DIN 02451182, held by JANSSEN INC, supplied as TABLET for ORAL administration. Health Canada currently lists it as marketed, status dated 23-Mar-2020. Nexara Health is a licensed Canadian wholesale distributor (DEL 3-002896-A) and can source this product for hospitals, pharmacies and clinics. Availability and lead time are confirmed per order.

What is UPTRAVI used for?

UPTRAVI® (selexipag) is indicated for the long-term treatment of idiopathic pulmonary arterial hypertension (iPAH), heritable pulmonary arterial hypertension (HPAH), PAH associated with connective tissue disorders and PAH associated with congenital heart disease, in adult patients with WHO functional class (FC) II – III to delay disease progression. Disease progression included: hospitalization for PAH, initiation of intravenous or subcutaneous prostanoids, or other disease progression events (decrease of 6-minute walk distance [6MWD] associated with either worsened PAH symptoms or need for additional PAH-specific treatment). UPTRAVI® is effective in combination with an endothelin receptor antagonist (ERA) or a phosphodiesterase-5 (PDE-5) inhibitor, or in triple combination with an ERA and a PDE-5 inhibitor, or as monotherapy.

Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.

How much does Selexipag cost around the world?

Selexipag is listed on 13 of the national price registers Nexara ingests. Each country publishes on a different basis, so those figures are not comparable with one another — or with a Canadian wholesale price.

What a market publishes matters more than the number it publishes. Australia publishes a ex-manufacturer; Bahrain publishes a retail (max); Czechia publishes a max producer price (ex-factory). Comparing an ex-factory ceiling against a pharmacy public price tells you nothing about either, and comparing either against a Canadian landed cost tells you less.

MarketPrice basis published thereBrandsPacks listedRange
Australiaex-manufacturer120AUD███.██
Czechiamax producer price (ex-factory)218CZK███.██
Saudi Arabiapublic912SAR███.██
United Arab Emiratespublic89AED███.██
Greeceproducer price (ex-factory)99EUR███.██
Italyprezzo al pubblico (classe A)99EUR███.██
Luxembourgreimbursement99EUR███.██
Romaniamax producer price89RON███.██
Slovakiacategorised final price89EUR███.██
South Africasingle exit price19ZAR███.██
Hungaryproducer price (ex-factory)88HUF███.██
Bahrainretail (max)16BHD███.██
Icelandmax wholesale15ISK███.██

132 pack listings across 74 brand entries and 11 price bases, refreshed 08 Sep 2026. Ranges span every Selexipag pack in that market, so a high figure is usually a larger pack rather than the same product.

Figures are held for the Nexara team. Cross-market prices are published on incompatible bases and are not an offer, a landed cost, or a guide to what any buyer can obtain. Nexara publishes which markets list the product and on what basis; the numbers stay internal.

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Canada publishes no comparable public list price. For a delivered Canadian price on a licensed account, verify your licence — it takes about a minute.

Ask Nexara for a landed Canadian price

Is there a generic Selexipag in Canada, and who makes it?

Every market authorization holder with a Canadian DIN for this molecule, and how many of their listings Health Canada currently shows as marketed.

Only one market authorization holder has a Canadian DIN containing Selexipag — 8 DINs, of which 8 are currently marketed. There is no second Canadian source today, so a supply interruption on this holder has no domestic substitute at the same molecule.

Market authorization holderDINsMarketedBrand namesPosition
JANSSEN INC88UPTRAVISourceable in Canada

Health Canada’s Drug Product Database does not flag which listing is the originator and which are subsequent-entry products, so Nexara does not label them here. Interchangeability is determined provincially, not federally — confirm for your province before a formulary switch. Nexara can confirm which of these is actually obtainable, and on what lead time, per order.

How is it supplied and stored?

Pack configuration, storage class and the handling constraints that drive cold-chain planning. One DIN can cover more than one pack size, and the pack — not the DIN — is what gets priced, shipped and invoiced.

Strength on the label800 MCG
Dosage formTABLET
RouteORAL
Pack configuration (monograph)60 film-coated tablets
Storagenull

Before an order line is unambiguous Nexara needs the strength, the pack size and the presentation.

Substance and classification

Active substanceSelexipag
ATC codeB01AC27
AHFS class48:48.00
Biosimilar biologicNo

Confirm the pack and get a price

Health Canada record and identifiers

The regulatory facts straight from the Drug Product Database, plus every identifier form Nexara accepts on a purchase order. A DIN written without its leading zeros is the commonest reason an order line fails to match.

DIN (8-digit, as used in ordering)02451182
DIN (unpadded, as printed on some documents)2451182
Brand nameUPTRAVI
Generic / active ingredientSELEXIPAG : 800 MCG
Market authorization holderJANSSEN INC
Health Canada schedulePrescription
ATC codeB01AC27
ATC anatomical main groupB — Blood and blood-forming organs
ATC therapeutic subgroupB01AC
Current statusMARKETED
Status date23-Mar-2020
Original market date2016-04-21 00:00:00
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record Approved product monograph (PDF)

What can be used instead?

Alternatives on every axis a buyer actually considers — the same molecule in another presentation, the same class, an adjacent class, or a fixed-dose combination. Every row is led by the marketed DIN count, because that is what can be bought this week.

1 · Same molecule, other Canadian presentations

8 of 8 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.

ProductStrengthFormHolderHealth Canada statusDIN
UPTRAVI200 MCGTABLETJANSSEN INCMARKETED02451158
UPTRAVI400 MCGTABLETJANSSEN INCMARKETED02451166
UPTRAVI600 MCGTABLETJANSSEN INCMARKETED02451174
UPTRAVI1000 MCGTABLETJANSSEN INCMARKETED02451190
UPTRAVI1200 MCGTABLETJANSSEN INCMARKETED02451204
UPTRAVI1400 MCGTABLETJANSSEN INCMARKETED02451212
UPTRAVI1600 MCGTABLETJANSSEN INCMARKETED02451220

2 · Same class — other molecules in ATC B01AC

MoleculeCanadian brandsDINsMarketedSourceable
ClopidogrelABBOTT-CLOPIDOGREL · ACCEL-CLOPIDOGREL · ACT CLOPIDOGREL · AG-CLOPIDOGREL · +22 more3919Yes
Acetylsalicylic AcidAPO-ASA LD · ASA · ASA 81 MG · ASA DAILY LOW DOSE · +17 more2312Yes
TicagrelorAG-TICAGRELOR · APO-TICAGRELOR · BRILINTA · JAMP TICAGRELOR · +3 more1412Yes
SelexipagUPTRAVI88Yes
TreprostinilREMODULIN · TREPROSTINIL INJECTION84Yes
EpoprostenolCARIPUL · EPOPROSTENOL FOR INJECTION · FLOLAN64Yes
DipyridamoleAPO-DIPYRIDAMOLE · APO-DIPYRIDAMOLE-SC TAB 25MG · APO-DIPYRIDAMOLE-SC TAB 50MG · APO-DIPYRIDAMOLE-SC TAB 75MG · +17 more242Yes
EptifibatideEPTIFIBATIDE INJECTION · INTEGRILIN142Yes
TirofibanAGGRASTAT21Yes
PrasugrelEFFIENT · JAMP PRASUGREL21Yes

A molecule with zero marketed DINs cannot be sourced domestically, however many approvals it holds — if one of these sits on a formulary or in an older protocol, that is the line to check.

3 · Adjacent classes in ATC B01A

ATC subgroupMoleculesDINsMarketed
B01AFApixaban · Edoxaban · Rivaroxaban159121
B01ABAntithrombin · Dalteparin · Danaparoid · Enoxaparin · Heparin · +3 more12882
B01AAAcenocoumarol · Warfarin6216
B01AEArgatroban · Bivalirudin · Dabigatran Etexilate · Lepirudin1811
B01AXCaplacizumab · Defibrotide · Fondaparinux105
B01ADAlteplase · Ancrod · Anistreplase · Drotrecogin Alfa · Reteplase · +3 more224

Not clinical advice. These tables describe what can be supplied in Canada, not what should be prescribed. Substitution within or across classes is a prescriber and pharmacist decision, and interchangeability is determined provincially.

What else is UPTRAVI called?

The same molecule, Selexipag, is registered under other names elsewhere. Buyers and prescribers searching from outside Canada — or working from a foreign prescription or tender document — often know it by one of these:

NameScriptRegistered in
SELEXIPAG ACCORDLatinCzechia
UPTRAVI®LatinSouth Africa
LexipiaLatinSaudi Arabia

Names are taken from national medicine registers and published price lists. A product registered abroad is not authorized for sale in Canada unless it holds its own DIN; import is possible only through the routes Health Canada permits.

How can I get it?

Nexara Health supplies this product to licensed Canadian buyers — pharmacies, hospitals, clinics, licensed distributors, and clinical trial sponsors or their CROs. We confirm stock, pack size, expiry and pricing at the time of quotation. If the product is on backorder or in shortage, we identify equivalent alternatives and import options where permitted.

Request a quote for UPTRAVI

Ordering questions

Who can buy this from Nexara?

Licensed entities only. Nexara holds Health Canada establishment licence DEL 3-002896-A and ships only to a licensed address. Patients and unlicensed buyers are routed to a partner pharmacy.

Is there a minimum order?

Yes, set per product line and per pack multiple rather than on the order total, so you are never asked to buy a part-pack. The minimum for this line is confirmed with your quote.

What is the lead time?

Confirmed per order at quotation, and it depends on current stock position and whether the product is in shortage.

Why is there no price on this page?

Nexara quotes a delivered Canadian price per order, against a verified licence. Foreign list prices are published on incompatible bases and are not a guide to what any buyer can obtain here, so this page shows which markets list the molecule and on what basis, and nothing more.

Can Nexara supply this for a clinical trial?

Yes — comparator and background-therapy supply, including sourcing from other markets where a Canadian pack will not satisfy the protocol. Clinical trial supply.

Sources and disclaimer

Product data sourced from the Health Canada Drug Product Database and the approved product monograph (PDF). Health Canada status reconciled against the live DPD sync. Last reviewed 10 Sep 2026.

Nothing on this page is medical advice. Nexara Health is a licensed wholesale distributor and supplies licensed entities only; consumer orders are routed to a partner pharmacy. Alternatives tables describe supply, not clinical equivalence.

Health Canada Drug Product Database (DPD), DIN 02451182. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.